Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP722932.RA40tfKNx-9hzh8jMtqDcEUs5ybHOkqP8aVZFcCR_GpNs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP722932.RA40tfKNx-9hzh8jMtqDcEUs5ybHOkqP8aVZFcCR_GpNs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP722932.RA40tfKNx-9hzh8jMtqDcEUs5ybHOkqP8aVZFcCR_GpNs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP722932.RA40tfKNx-9hzh8jMtqDcEUs5ybHOkqP8aVZFcCR_GpNs130_provenance.
- NP722932.RA40tfKNx-9hzh8jMtqDcEUs5ybHOkqP8aVZFcCR_GpNs130_assertion description "[Chordin is a modifier of tbx1 for the craniofacial malformations of 22q11 deletion syndrome phenotypes in mouse.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP722932.RA40tfKNx-9hzh8jMtqDcEUs5ybHOkqP8aVZFcCR_GpNs130_provenance.
- NP722932.RA40tfKNx-9hzh8jMtqDcEUs5ybHOkqP8aVZFcCR_GpNs130_assertion evidence source_evidence_literature NP722932.RA40tfKNx-9hzh8jMtqDcEUs5ybHOkqP8aVZFcCR_GpNs130_provenance.
- NP722932.RA40tfKNx-9hzh8jMtqDcEUs5ybHOkqP8aVZFcCR_GpNs130_assertion SIO_000772 19247433 NP722932.RA40tfKNx-9hzh8jMtqDcEUs5ybHOkqP8aVZFcCR_GpNs130_provenance.
- NP722932.RA40tfKNx-9hzh8jMtqDcEUs5ybHOkqP8aVZFcCR_GpNs130_assertion wasDerivedFrom befree-2016 NP722932.RA40tfKNx-9hzh8jMtqDcEUs5ybHOkqP8aVZFcCR_GpNs130_provenance.
- NP722932.RA40tfKNx-9hzh8jMtqDcEUs5ybHOkqP8aVZFcCR_GpNs130_assertion wasGeneratedBy ECO_0000203 NP722932.RA40tfKNx-9hzh8jMtqDcEUs5ybHOkqP8aVZFcCR_GpNs130_provenance.
- befree-2016 importedOn "2016-02-19" NP722932.RA40tfKNx-9hzh8jMtqDcEUs5ybHOkqP8aVZFcCR_GpNs130_provenance.